Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB)

Prenatal Diagnosis

Volumn 21, Issue 12, 2001, Pages 1049-1052

  Starke, Heike ^a,b   Senger, Gabriele ^c,d   Kossakiewicz, Maria ^a   Tittelbach, Hanne ^a   Rau, Dorothea ^a   Rubtsov, Nikolai ^a   Trifonov, Vladimir ^a   Heller, Anita ^a,b   Hartmann, Isabell ^a   Claussen, Uwe ^a   Liehr, Thomas ^a,d  

^a Institute of Human Genetics and Anthropology   (Germany)

^b Practice of Medical Genetics and Gynaecology   (Germany)

^c Practice of Human Genetics   (Germany)

^d INSTITUTE OF CYTOLOGY AND GENETICS   (Russian Federation)

Author keywords

Chromosome 18; Insertion; Microdissection; Multicolour banding

Indexed keywords

AMNIOCENTESIS; ARTICLE; CASE REPORT; CHROMOSOME 18Q; CHROMOSOME ABERRATION; CHROMOSOME MICRODISSECTION; CYTOGENETICS; FETUS; GENE INSERTION; HUMAN; KARYOTYPING; PARTIAL MONOSOMY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ADULT; AMNIOTIC FLUID; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 18; CYTOGENETIC ANALYSIS; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MUTAGENESIS, INSERTIONAL; PREGNANCY; PRENATAL DIAGNOSIS;

INSERTION SEQUENCES;

EID: 0035684344     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.192     Document Type: Article

References (22)

1. Adenomatous polyposis coli and a cytogenetic deletion of chromosome 5 resulting from a maternal intrachromosomal insertion
2. Divergent outcomes of intrachromosomal recombination on the human Y chromosome: Male infertility and recurrent polymorphism
3. Familial mental retardation in a family with an inherited chromosome rearrangement
4. High resolution multicolor-banding: A new technique for refined FISH analysis of human chromosomes
5. Cri-du-chat syndrome and two other deformed children in a family carrying a pericentric inversion or insertion of chromosome 5
6. Familial partial distal 18q (18q22-18q23) trisomy
7. Partial trisomy 4p resulting from a balanced intrachromosomal insertion, 4(q313p14p16)
8. Regional localization of 10 mariner transposon-like ESTs by means of FISH - Evidence for a correlation with fragile sites
9. Intrachromosomal insertions: A case report and a review
10. Duplication 5q(5q22-q33): From an intrachromosomal insertion
11. Partial trisomy 4 resulting from a complex maternal rearrangement of chromosomes 2, 4, and 18 with interstitial translocation
12. Meiotic consequences of an intrachromosomal insertion of chromosome no. 1: A family pedigree
13. Partial trisomy 1 (1q31-q41) caused by intrachromosomal insertion in 1p31.3 in a newborn infant and a sister of the mother
14. Localization of mariner DNA transposons in the human genome by PRINS
15. Molecular evolution of the second ancient human transposon. Hsmar2, illustrates patterns of neutral evolution in the human genome lineage
16. Ocular albinism in a male with del (6)(q13-q15): Candidate region for autosomal recessive ocular albinism?
17. Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection
18. Karyotyping human chromosomes by combinatorial multi-fluor FISH
19. A complex five breakpoint intrachromosomal rearrangement ascertained through two recombinant offspring
20. Interchromosomal insertions Identification of five cases and a review
21. Duplication of the long arm of chromosome 13 secondary to a recombination in a maternal intrachromosomal insertion (shift)